5300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes 6.0-10.0mm; 5310600-5311000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, Fenestrated, sizes 6.0-10.0mm; 5400600-5401000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, sizes 6.0-10.0mm; 5410500-5411000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, Fenestrated, sizes 6.0-10.0mm
K242921 is the FDA 510(k) clearance record for 5300600-5301000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, sizes 6.0-10.0mm; 5310600-5311000 Rota-Trach Disposable Standard Tracheostomy Tube, Cuffed, Fenestrated, sizes 6.0-10.0mm; 5400600-5401000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, sizes 6.0-10.0mm; 5410500-5411000 Rota-Trach Disposable Standard Tracheostomy Tube, Uncuff, Fenestrated, sizes 6.0-10.0mm, a class II device, cleared for Vitaltec Corporation on under FDA product code BTO (Tube, Tracheostomy (W/Wo Connector)). FDA records list 2 510(k) clearances for Vitaltec Corporation, from to . As of , FDA records show no recalls naming K242921.
Clearance record
- Decision date
- Received
- (259 days to decision)
- Product code
- BTO Tube, Tracheostomy (W/Wo Connector)
- Regulation
- 21 CFR 868.5800
- Device class
- Class II
- Review panel
- Anesthesiology
- Applicant
- Vitaltec Corporation # 12, Ln. 4-30, Chyuan-Zhou Rd., Hou-Li Dist., Taichung City, TW
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code BTO
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
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